Suppr超能文献

活化白细胞细胞黏附分子刺激过敏性哮喘中的 T 细胞反应。

Activated Leukocyte Cell Adhesion Molecule Stimulates the T-Cell Response in Allergic Asthma.

机构信息

1 Department of Pediatrics.

2 Institute of Allergy.

出版信息

Am J Respir Crit Care Med. 2018 Apr 15;197(8):994-1008. doi: 10.1164/rccm.201703-0532OC.

Abstract

RATIONALE

The activated leukocyte cell adhesion molecule (ALCAM) is a cluster of differentiation 6 ligand that is important for stabilizing the immunological synapse and inducing T-cell activation and proliferation.

OBJECTIVES

In this study, we investigated the role of ALCAM in the development of inflammation in allergic asthma.

METHODS

An ovalbumin (OVA)-induced allergic asthma model was established in wild-type (WT) and ALCAM-deficient (ALCAM) mice. T-cell proliferation was evaluated in cocultures with dendritic cells (DCs). Bone marrow-derived dendritic cells (BMDCs) from WT and ALCAM mice were cultured and adoptively transferred to OT-II mice for either OVA sensitization or challenge. An anti-ALCAM antibody was administered to assess its therapeutic potential. ALCAM concentrations in the sputum and serum of children with asthma were quantified by ELISA.

MEASUREMENTS AND MAIN RESULTS

Inflammatory responses were lower in ALCAM mice than in WT mice, and T cells cocultured with DCs from ALCAM mice showed reduced proliferation relative to those cocultured with DCs from WT mice. A decreased inflammatory response was observed upon adoptive transfer of BMDCs from ALCAM mice as compared with that observed after transfer of BMDCs from WT mice. In addition, anti-ALCAM antibody-treated mice showed a reduced inflammatory response, and sputum and serum ALCAM concentrations were higher in children with asthma than in control subjects.

CONCLUSIONS

ALCAM contributes to OVA-induced allergic asthma by stimulating T-cell activation and proliferation, suggesting it as a potential therapeutic target for allergic asthma.

摘要

背景

活性白细胞细胞黏附分子(ALCAM)是分化群 6 配体的一个簇,对于稳定免疫突触和诱导 T 细胞活化和增殖非常重要。

目的

本研究旨在探讨 ALCAM 在过敏性哮喘炎症发展中的作用。

方法

建立野生型(WT)和 ALCAM 缺陷型(ALCAM)小鼠卵清蛋白(OVA)诱导的过敏性哮喘模型。通过与树突状细胞(DC)共培养评估 T 细胞增殖。培养 WT 和 ALCAM 小鼠的骨髓来源树突状细胞(BMDC),并将其过继转移至 OT-II 小鼠进行 OVA 致敏或激发。给予抗-ALCAM 抗体以评估其治疗潜力。通过 ELISA 定量检测哮喘儿童痰和血清中的 ALCAM 浓度。

测量和主要结果

与 WT 小鼠相比,ALCAM 小鼠的炎症反应较低,与 WT 小鼠来源的 DC 共培养的 T 细胞增殖减少。与 WT 小鼠来源的 BMDC 过继转移相比,ALCAM 小鼠来源的 BMDC 过继转移观察到炎症反应降低。此外,用抗-ALCAM 抗体治疗的小鼠炎症反应减轻,哮喘儿童的痰和血清中 ALCAM 浓度高于对照组。

结论

ALCAM 通过刺激 T 细胞的活化和增殖促进 OVA 诱导的过敏性哮喘,表明其可能成为过敏性哮喘的潜在治疗靶点。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验